S-adenosyl-L-methionine for treatment of depression, osteoarthritis, and liver disease
Hardy M, Coulter I, Morton SC
            Record ID 32003000428
            English
                                    
                Authors' objectives:
                
                                    This report is a comprehensive literature review and synthesis of evidence on the use of S-adenosyl-L-methionine (SAMe) for the treatment of depression, osteoarthritis, and liver disease.
                Authors' results and conclusions:
                - Compared to placebo, treatment with SAMe was associated with an improvement of approximately 6 points in the score of the Hamilton Rating Scale for Depression. (This degree of improvement is clinically significant and is equivalent to a partial response to treatment.)
- Compared to treatment with conventional therapy, SAMe was not associated with a statistically significant difference in outcomes.
- Compared to placebo for osteoarthritis, one large randomized clinical trial showed a small to moderate effect in favor of SAMe.
- Compared to nonsteroidal anti-inflammatory agents, treatment with SAMe was not associated with a statistically significant difference in outcomes.
- Compared to placebo, treatment with SAMe for cholestasis of pregnancy was associated with a large effect in decreasing pruritus and in decreasing bilirubin levels.
- In two clinical trials for cholestasis of pregnancy, conventional therapy (ursodeoxycholic acid) was favored over SAMe for the treatment of pruritus.
- Compared to placebo for intrahepatic cholestasis, treatment with SAMe for pruritus was associated with a risk ratio of 0.45, meaning that patients treated with SAMe were twice as likely as placebo-treated patients to have a reduction in pruritus (95% CI [0.37, 0.58]).
- Too few studies compared SAMe to active therapy for intrahepatic cholestasis to conduct a pooled analysis.
- Twenty remaining studies were too heterogeneous with respect to diagnosis (a wide variety of liver conditions) and outcomes to permit pooled analysis.
            
                                    
                Authors' recommendations:
                These data indicate that SAMe is more effective than placebo for relief of symptoms of depression, pain of osteoarthritis, and pruritus in cholestasis of pregnancy, and in intrahepatic cholestasis. SAMe is more effective than placebo in reducing bilirubin for cholestasis of pregnancy and serum bilirubin for intrahepatic cholestasis. Treatment with SAMe was equivalent to standard therapy for depression and osteoarthritis but not for liver disease.
These results justify additional randomized controlled trials to evaluate the efficacy and tolerability of SAMe for treatment of depression, osteoarthritis, and cholestasis (related to pregnancy and associated with other liver diseases).
            
                                    
                Authors' methods:
                Systematic review
            
                        
            Details
                        
                Project Status:
                Completed
            
                                    
                URL for project:
                http://www.ahrq.gov/clinic/tp/sametp.htm
            
                                                
                Year Published:
                2002
            
                                                                        
                English language abstract:
                An English language summary is available
            
                                    
                Publication Type:
                Not Assigned
            
                                    
                Country:
                United States
            
                                                
                        MeSH Terms
            - S-Adenosylmethionine
- Depression
- Liver Diseases
- Osteoarthritis
Contact
                        
                Organisation Name:
                Agency for Healthcare Research and Quality
            
            
                        
                Contact Address:
                Center for Outcomes and Evidence Technology Assessment Program, 540 Gaither Road, Rockville, MD 20850, USA. Tel: +1 301 427 1610; Fax: +1 301 427 1639;
            
                                    
                Contact Name:
                martin.erlichman@ahrq.hhs.gov
            
                                    
                Contact Email:
                martin.erlichman@ahrq.hhs.gov
            
                                    
                Copyright:
                Agency for Healthcare Research and Quality (AHRQ)
            
                    
                This is a bibliographic record of a published health technology assessment from a member of INAHTA or other HTA producer. No evaluation of the quality of this assessment has been made for the HTA database.